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G71 Primary disorders of muscles

ICD-10-CM category G71 sits in Chapter 6 (Diseases of the nervous system, G00-G99). It contains 28 billable codes for FY2027, effective October 1, 2026 to September 30, 2027. Always code to the most specific code available: a code with more characters that describes the diagnosis more precisely takes priority over a shorter one.

Subcategories

G71.0 Muscular dystrophyG71.03 Limb girdle muscular dystrophiesG71.034 Limb girdle musc dyst due to sarcoglycan dysfunctionG71.1 Myotonic disordersG71.2 Congenital myopathiesG71.22 Centronuclear myopathy

Billable codes in G71

CodeDescription
G71.00Muscular dystrophy, unspecified
G71.01Duchenne or Becker muscular dystrophy
G71.02Facioscapulohumeral muscular dystrophy
G71.031Autosomal dominant limb girdle muscular dystrophy
G71.032Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
G71.033Limb girdle muscular dystrophy due to dysferlin dysfunction
G71.0340Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecified
G71.0341Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
G71.0342Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
G71.0349Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
G71.035Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
G71.036Limb girdle muscular dystrophy due to fukutin related protein dysfunction
G71.038Other limb girdle muscular dystrophy
G71.039Limb girdle muscular dystrophy, unspecified
G71.09Other specified muscular dystrophies
G71.11Myotonic muscular dystrophy
G71.12Myotonia congenita
G71.13Myotonic chondrodystrophy
G71.14Drug induced myotonia
G71.19Other specified myotonic disorders
G71.20Congenital myopathy, unspecified
G71.21Nemaline myopathy
G71.220X-linked myotubular myopathy
G71.228Other centronuclear myopathy
G71.29Other congenital myopathy
G71.3Mitochondrial myopathy, not elsewhere classified
G71.8Other primary disorders of muscles
G71.9Primary disorder of muscle, unspecified

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